Why VaLogic? A Trusted Partner for Compliance
Choosing the right partner for GxP compliance is critical to meeting regulatory standards and keeping your operations running smoothly. With deep industry expertise and a proven track record, VaLogic is your trusted provider.
- 150+ years of combined experience across CGMP compliance, quality systems management, and risk-based validation
- Tailored GxP solutions that address the unique challenges of life science companies
- Extensive knowledge of USP <795>, <797>, <800>, and 503A and 503B compounding standards
- Full-time, in-house validation technicians
- Millions invested in state-of-the-art equipment
Comprehensive GxP Consulting Services for Every Stage
Solutions that fit your company size, stage, and goals.
We provide end-to-end GxP consulting services to support your business from early-stage development to commercial production.
GxP Consulting for Early-Phase & Clinical Trials
- Risk-based facility assessments to ensure your operations are compliant from the start
- Process validation planning to guide you through developing and validating critical processes
- CMC regulatory submissions support to ensure timely, accurate submissions
Commercial Production Compliance & Ongoing Support
- GxP audits to ensure ongoing compliance during trials and production
- Cleanroom certification to maintain stringent regulatory requirements for contamination control
- Calibration services for critical equipment to ensure precise performance
- Validation services for accuracy and reliability of processes and systems
Core GxP Consulting Services
- CGMP compliance to meet or exceed all current good manufacturing practices
- Risk-based validationsto align with GMP, USP <795>, USP <797>, USP <800>, 503A vs 503B, and other regulatory standards, ensuring compliance.
- Inspection readiness for FDA and regulatory audits
- Quality systems management & troubleshooting to optimize and maintain quality systems that mitigate risks
